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MRI demonstrates glutamine antagonist-mediated reversal of cerebral malaria pathology in mice
Author(s) -
Brittany A. Riggle,
Sanhita Sinharay,
William Schreiber-Stainthorp,
Jeeva Munasinghe,
Dragan Maric,
Eva Prchalová,
Barbara S. Slusher,
Jonathan D. Powell,
Louis H. Miller,
Susan K. Pierce,
Dima A. Hammoud
Publication year - 2018
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1812909115
Subject(s) - glutamine , antagonist , pathology , cerebral malaria , malaria , medicine , pharmacology , chemistry , plasmodium falciparum , biochemistry , amino acid , receptor
The deadliest complication of Plasmodium falciparum infection is cerebral malaria (CM), with a case fatality rate of 15 to 25% in African children despite effective antimalarial chemotherapy. No adjunctive treatments are yet available for this devastating disease. We previously reported that the glutamine antagonist 6-diazo-5-oxo-l-norleucine (DON) rescued mice from experimental CM (ECM) when administered late in the infection, a time by which mice had already suffered blood-brain barrier (BBB) dysfunction, brain swelling, and hemorrhaging. Herein, we used longitudinal MR imaging to visualize brain pathology in ECM and the impact of a new DON prodrug, JHU-083, on disease progression in mice. We demonstrate in vivo the reversal of disease markers in symptomatic, infected mice following treatment, including the resolution of edema and BBB disruption, findings usually associated with a fatal outcome in children and adults with CM. Our results support the premise that JHU-083 is a potential adjunctive treatment that could rescue children and adults from fatal CM.

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